Evidence map›Paper›PMID 38396713›Full record

ArticleInternational journal of molecular sciences2024

Does Telotristat Have a Role in Preventing Carcinoid Heart Disease?

Aura D Herrera-Martínez, Antonio C Fuentes-Fayos, Rafael Sanchez-Sanchez, Antonio J Montero, André Sarmento-Cabral, María A Gálvez-Moreno, Manuel D Gahete, Raúl M Luque

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Aura D Herrera-MartínezMaimonides Institute for Biomedical Research of Cordoba (IMIBIC), 14004 Córdoba, Spain.ORCID 0000-0003-1437-9878
Antonio C Fuentes-FayosMaimonides Institute for Biomedical Research of Cordoba (IMIBIC), 14004 Córdoba, Spain.ORCID 0000-0003-2069-4823
Rafael Sanchez-SanchezMaimonides Institute for Biomedical Research of Cordoba (IMIBIC), 14004 Córdoba, Spain.ORCID 0000-0002-9497-2315
Antonio J MonteroMaimonides Institute for Biomedical Research of Cordoba (IMIBIC), 14004 Córdoba, Spain.
André Sarmento-CabralMaimonides Institute for Biomedical Research of Cordoba (IMIBIC), 14004 Córdoba, Spain.ORCID 0000-0002-1204-0371
María A Gálvez-MorenoMaimonides Institute for Biomedical Research of Cordoba (IMIBIC), 14004 Córdoba, Spain.
Manuel D GaheteMaimonides Institute for Biomedical Research of Cordoba (IMIBIC), 14004 Córdoba, Spain.ORCID 0000-0002-4578-2179
Raúl M LuqueMaimonides Institute for Biomedical Research of Cordoba (IMIBIC), 14004 Córdoba, Spain.ORCID 0000-0002-7585-1913
Spanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ES

Funding

GETNE Junior Research Award 2019 GETNE Junior Research Award 2019Instituto de Salud Carlos III JR/00050
6 · The paper itself

Abstract

Carcinoid heart disease (CHD) is a frequent and life-threatening complication in patients with carcinoid tumors. Its clinical management is challenging is some cases since serotonin-induced valve fibrosis leads to heart failure. Telotristat is an inhibitor of tryptophan-hydroxylase (TPH), a key enzyme in serotonin production. Telotristat use in patients with carcinoid syndrome and uncontrollable diarrhea under somatostatin analogs is approved, but its specific role in patients with CHD is still not clear. IN this context, we aimed to explore the effect of telotristat in heart fibrosis using a mouse model of serotonin-secreting metastasized neuroendocrine neoplasm (NEN). To this aim, four treatment groups (n = 10/group) were evaluated: control, monthly octreotide, telotristat alone, and telotristat combined with octreotide. Plasma serotonin and NT-proBNP levels were determined. Heart fibrosis was histologically evaluated after 6 weeks of treatment or when an individual mouse's condition was close to being terminal. Heart fibrosis was observed in all groups. Non-significant reductions in primary tumor growth were observed in all of the treated groups. Feces volume was increased in all groups. A non-significant decrease in feces volume was observed in the octreotide or telotristat-treated groups, while it was significantly reduced with the combined treatment at the end of the study compared with octreotide (52 g reduction;

Indexed as

Carcinoid Heart DiseaseNeuroendocrine TumorsPyrimidinesFibrosisHumansOctreotidePhenylalanineSerotoninOctreotidePhenylalaninePyrimidinesSerotonintelotristatcarcinoid heart diseaseserotonintelotristat

Identifiers

PMID38396713
PMCPMC10888480
OpenAlexW4391601339

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.